PQS and pyochelin in Pseudomonas aeruginosa share inner membrane transporters to mediate iron uptake

• Published in: Microbiology spectrum 2024-02, Vol.12 (2), p.e0325623-e0325623
• Main Authors: Zhang, Heng, Yang, Jianshe, Cheng, Juanli, Zeng, Jing, Ma, Xin, Lin, Jinshui
• Format: Article
• Language: English
• Subjects: Bacterial Outer Membrane Proteins - metabolism; Bacterial Proteins - metabolism; Bacteriology; inner membrane transporter; Iron - metabolism; iron uptake; Membrane Transport Proteins - metabolism; Phenols; PQS; Pseudomonas aeruginosa; Pseudomonas aeruginosa - genetics; pyochelin; Quinolones; Receptors, Cell Surface - metabolism; Research Article; Siderophores - metabolism; Thiazoles
• ISSN: 2165-0497; 2165-0497
• DOI: 10.1128/spectrum.03256-23

Bacteria absorb different forms of iron through various channels to meet their needs. Our previous studies have shown that TseF, a type VI secretion system effector for Fe uptake, facilitates the delivery of outer membrane vesicle-associated quinolone signal (PQS)-Fe to bacterial cells by a process involving the Fe(III) pyochelin receptor FptA and the porin OprF. However, the form in which the PQS-Fe complex enters the periplasm and how it is moved into the cytoplasm remain unclear. Here, we first demonstrate that the PQS-Fe complex enters the cell directly through FptA or OprF. Next, we show that inner membrane transporters such as FptX, PchHI, and FepBCDG are not only necessary for to absorb PQS-Fe and pyochelin (PCH)-Fe but are also necessary for the virulence of toward larvae. Furthermore, we suggest that the function of PQS-Fe (but not PQS)-mediated quorum-sensing regulation is dependent on FptX, PchHI, and FepBCDG. Additionally, the findings indicate that unlike FptX, neither FepBCDG nor PchHI play roles in the autoregulatory loop involving PchR, but further deletion of and can reverse the inactive PchR phenotype caused by deletion and reactivate the expression of the PCH pathway genes under iron-limited conditions. Finally, this work identifies the interaction between FptX, PchHI, and FepBCDG, indicating that a larger complex could be formed to mediate the uptake of PQS-Fe and PCH-Fe . These results pave the way for a better understanding of the PQS and PCH iron absorption pathways and provide future directions for research on tackling infections.IMPORTANCE has evolved a number of strategies to acquire the iron it needs from its host, with the most common being the synthesis, secretion, and uptake of siderophores such as pyoverdine, pyochelin, and the quorum-sensing signaling molecule quinolone signal (PQS). However, despite intensive studies of the siderophore uptake pathways of , our understanding of how siderophores transport iron across the inner membrane into the cytoplasm is still incomplete. Herein, we reveal that PQS and pyochelin in share inner membrane transporters such as FptX, PchHI, and FepBCDG to mediate iron uptake. Meanwhile, PQS and pyochelin-mediated signaling operate to a large extent via these inner membrane transporters. Our study revealed the existence of shared uptake pathways between PQS and pyochelin, which could lead us to reexamine the role of these two molecules in the iron uptake and virulence of .